Clinical outcome with low-dose valacyclovir in high-risk renal transplant recipients: a 10-year experience
Author(s) -
Fredrik Sund,
Gunnar Tufveson,
Bernd Döhler,
Gerhard Opelz,
BrittMarie Eriksson
Publication year - 2012
Publication title -
nephrology dialysis transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.654
H-Index - 168
eISSN - 1460-2385
pISSN - 0931-0509
DOI - 10.1093/ndt/gfs531
Subject(s) - medicine , renal transplant , adverse effect , transplantation , gastroenterology
Cytomegalovirus (CMV) remains an important pathogen in transplant patients, and valacyclovir (VACV) prophylaxis 8 g/day has been used in high-risk CMV-seromismatched [D+/R-] renal transplant patients to decrease CMV disease. Neurotoxic adverse effects have limited its use, and the aim of the present study was to retrospectively evaluate low-dose VACV prophylaxis, 3 g/day for 90 days after transplantation, in 102 D+/R- renal transplant patients.
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